The Use of Ceftaroline as Surgical Prophylaxis in Surgery With Risk of MRSA Infection — PREVTAROLINE  

Surgical Site Infection Clinical Trial

Official title: IDC 56: A Randomized Double-blinded Study Comparing Ceftaroline to Standard of Care Therapy With Cefazolin and Vancomycin as Surgical Prophylaxis for High Risk Orthopedic and Cardiac Surgeries

Status Recruiting

Clinical Trial Summary

The study is a randomized double-blinded study comparing ceftaroline to standard of care therapy with cefazolin and vancomycin as surgical prophylaxis for high risk orthopedic and cardiac surgeries. Study participants will be enrolled from those undergoing cardiothoracic surgery involving sternotomy and those undergoing prosthetic joint replacement of either hip or knee. Consenting patients will be randomized 2:1 to receive either ceftaroline or cefazolin/vancomycin. This study will be blinded by the use of placebo vancomycin infusions and placebo cephalosporin infusions. The primary end point will be the development of a surgical site infection within 30 days of surgery.

Clinical Trial Description

The study is a randomized double-blinded study comparing ceftaroline to standard of care therapy with cefazolin and vancomycin as surgical prophylaxis for high risk orthopedic and cardiac surgeries. Study participants will be enrolled from those undergoing cardiothoracic surgery involving sternotomy and those undergoing prosthetic joint replacement of either hip or knee. Consenting patients will be randomized 2:1 to receive either ceftaroline or cefazolin/vancomycin. This study will be blinded by the use of placebo vancomycin infusions and placebo cephalosporin infusions. Study participants will be enrolled from 2 populations of patients; those undergoing cardiothoracic surgery with sternotomy and those undergoing prosthetic joint replacement of either hip or knee.

Subjects will be identified by the primary surgical service. Adult subjects 18 years and older will be notified of the study and if agreeable will be interviewed by a study coordinator who will explain the study and study procedures and determine eligibility. Informed consent will be obtained from potential participants. Enrollment and consent may be obtained up to seven days prior to surgery.

Consented participants will have a detailed history performed with particular reference to prior surgical infections, risk factors such as diabetes, smoking, prior skin infections and obesity. Participants will undergo a physical examination. Patients will be assessed for nares colonization with methicillin-resistant Staphylococcus aureus (MRSA) as per the primary surgeon's standard procedure. Patients identified as positive for MRSA colonization will be decolonized with mupirocin. Female participants will have a serum beta-human chorionic gonadotrophin (HCG) assay performed to exclude pregnancy.

Consented participants will be randomized 2:1 to receive either ceftaroline or cefazolin/vancomycin, the current regimen for high risk individuals. Randomization will be performed by a blinded individual using a randomization program. Within each group, participants will be allocated in the 2:1 ratio.

On the day of surgery, all patients will be evaluated for changes in medical history, vital signs recorded and bilateral nares swabs obtained for Staphylococcal screening for both MRSA and methicillin-sensitive Staphylococcus aureus (MSSA) carriage. All patients will receive pre-operative toweling of the operative site with chlorhexidine, and a surgical skin preparation of chlorhexidine/alcohol (Duraprep).

Consented participants will receive two blinded infusions. Study infusions will be prepared by an unblinded pharmacist to match the active medications. Placebo and study medication will be matched in volume and appearance. Dosing of vancomycin and cefazolin will be weight based up to 120 kg at 15 mg/kg and 25 mg/kg respectively. ceftaroline will be administered at a dose of 600 mg in individuals with estimated creatinine clearance of greater than 50 ml/min and 400 mg for those with creatinine clearance rates of 30-50 ml/min. Vancomycin or placebo1 will be started 120 minutes prior to incision and completed within 60 minutes prior to surgery. The cefazolin or ceftaroline will be started 60 minutes before surgery and completed 30 minutes prior to incision. Each participant will thus receive 2 infusions at T-120 and T-60 minutes from time of skin incision.

Patients will be redosed with antibiotics between 1.5 to 2 half-lives (cefazolin or ceftaroline at 4hrs hours post skin incision and vancomycin/placebo 1 at 12 hrs) in prolonged procedures. One post-operative dose of of cefazolin/ceftraroline will be given in the recovery room 4 hours after skin incision for those patients who were not redosed during the procedure for orthopedic procedures and 2 doses will be administered for cardiothoracic procedures.

Pharmacokinetic substudy:

Because of the variation in the pharmacokinetics previously identified for patients undergoing extracorporeal circulation, we will perform a pharmacokinetic analysis on a subset of 50 patients in the cardiac surgery arm of the study to allow data on at least 30 patient receiving ceftaroline. Plasma samples will be collected at the start of infusion (time = 0, Sample #1), end of infusion (time = 30 minutes, Sample #2), 15 minutes post infusion (Sample #3), at the time of skin incision (Sample #4) at commencement of cardiopulmonary bypass (CPB) (Sample # 5), at completion of CPB (Sample # 6) and at the time of skin closure (Sample #7). Samples will be analyzed by high pressure liquid chromatography (HPLC) to determine ceftaroline levels using known plasma standards with appropriate quality controls.

Patients will undergo a wound inspection by study personnel prior to discharge from hospital. Microbiological cultures will be obtained from all surgical site infections. All isolates will be reported out. Patients will be interviewed and examined at day 30 for the presence of evidence of surgical site infection at any operative site. Subjects will be questioned with regard to the presence of fever, redness or drainage or other manifestations of infection. Physical examination findings by the surgical team at prior post-operative visits will be reviewed and correlated with the data obtained from the subject. The primary end point will be the development of a surgical site infection within 30 days of surgery.

30 day surgical site infection rates at either the primary surgical site or any remote surgical site (e.g. vein donor site for CABG procedures) will be used as the principal outcome measure. Surgical site infections will be characterized as superficial (above the fascia) or complex (deep (extending below the fascia) and organ involving), Secondary endpoints recorded will include (i) other infections, viz. pulmonary, UTI, line related); (ii) Drug related, viz., rash, itching; and (iii) nausea, vomiting and (iiii) return to OR. ;

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Prevention

Related Conditions & MeSH terms

• Surgical Site Infection
• Surgical Wound Infection

• NCT number: NCT02307006
• Study type: Interventional
• Source: University of Cincinnati
• Contact: Alan G Smulian, M.B.B. Ch.
• Phone: 513 558-4248
• Email: smuliang@fuse.net
• Status: Recruiting
• Phase: Phase 4
• Start date: January 2015
• Completion date: June 2017